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Mechanism of the CO oxidation reaction on O-precovered Pt(111) surfaces studied with near-edge x-ray absorption fine structure spectroscopy.
Nakai, I; Kondoh, H; Amemiya, K; Nagasaka, M; Shimada, T; Yokota, R; Nambu, A; Ohta, T.
Affiliation
  • Nakai I; Department of Chemistry, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
J Chem Phys ; 122(13): 134709, 2005 Apr 01.
Article de En | MEDLINE | ID: mdl-15847491
ABSTRACT
The mechanism of CO oxidation reaction on oxygen-precovered Pt(111) surfaces has been studied by using time-resolved near-edge x-ray absorption fine structure spectroscopy. The whole reaction process is composed of two distinct paths (1) a reaction of isolated oxygen atoms with adsorbed CO, and (2) a reaction of island-periphery oxygen atoms after the CO saturation. CO coadsorption plays a role to induce the dynamic change in spatial distribution of O atoms, which switches over the two reaction paths. These mechanisms were confirmed by kinetic Monte Carlo simulations. The effect of coadsorbed water in the reaction mechanism was also examined.
Recherche sur Google
Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: J Chem Phys Année: 2005 Type de document: Article Pays d'affiliation: Japon
Recherche sur Google
Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: J Chem Phys Année: 2005 Type de document: Article Pays d'affiliation: Japon